Package 81964-575-83

{"route": ["ORAL"], "spl_id": "3854c6ad-10f7-dae3-e063-6294a90ae00a", "openfda": {"upc": ["0381964575835", "0381964221145", "0381964212037", "0381964212051"], "unii": ["Q42OMW3AT8", "804826J2HU"], "rxcui": ["562508", "617302", "617322"], "spl_set_id": ["c4a6deb5-0bcd-4fa3-b19b-a82fa1dd14f3"], "manufacturer_name": ["USAntibiotics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, COATED in 1 BOTTLE (81964-575-83)", "package_ndc": "81964-575-83", "marketing_start_date": "20250702"}], "brand_name": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "product_id": "81964-575_3854c6ad-10f7-dae3-e063-6294a90ae00a", "dosage_form": "TABLET, COATED", "pharm_class": ["Penicillin-class Antibacterial [EPC]", "Penicillins [CS]", "beta Lactamase Inhibitor [EPC]", "beta Lactamase Inhibitors [MoA]"], "product_ndc": "81964-575", "generic_name": "amoxicillin and clavulanate potassium", "labeler_name": "USAntibiotics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMOXICILLIN AND CLAVULANATE POTASSIUM", "active_ingredients": [{"name": "AMOXICILLIN", "strength": "875 mg/1"}, {"name": "CLAVULANATE POTASSIUM", "strength": "125 mg/1"}], "application_number": "NDA050720", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250702", "listing_expiration_date": "20261231"}